Memmert GmbH + Co.KG
DE-MF-000012127 · Germany · Schwabach
Memmert GmbH + Co.KG is registered in the European database on medical devices as a manufacturer, with 212 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 148 |
|---|---|
| Class IIb | 64 |
Most frequent device types declared: ICO105medX2, SF160, SF160plus, SF260X2, SF55X2.
Among these devices, 212 are declared active.
Catalogue references include IF160mplus, IF450bw, IF75mX2, IN260m, SF160, SF160plus.
European nomenclature codes declared: A030105, S9099, Z12030305, T030399, V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 212 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 212 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: Neither register. Memmert GmbH + Co.KG was not found in either the U.S. or the Canadian register.